Tetrahedron Letters p. 6501 - 6504 (1990)
Update date:2022-08-03
Topics:
Baures
Eggleston
Flisak
Gombatz
Lantos
Mendelson
Remich
Chiral substituted glycidic esters have been prepared from their corresponding chalcones via a two step procedure consisting of an asymmetric epoxidation mediated by a poly-L-leucine polymer, followed by a previously unreported Baeyer-Villiger oxidation. The regioselectivity of this latter procedure was found to depend on the aryl substituent.
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